Evidence map›Paper›PMID 39711720›Full record

ArticlemedRxiv : the preprint server for health sciences2024

PNEUMOCOCCAL SEROTYPE DISTRIBUTION AND COVERAGE OF EXISTING AND PIPELINE PNEUMOCOCCAL VACCINES.

Laura M King, Kristin L Andrejko, Miwako Kobayashi, Wei Xing, Adam L Cohen, Wesley H Self, J Jackson Resser, Cynthia G Whitney, Adrienne Baughman, Mai Kio and 4 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Laura M KingSchool of Public Health, University of California, Berkeley, Berkeley, California, United States.ORCID 0000-0002-7785-4712
Kristin L AndrejkoDivision of Bacterial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States.
Miwako KobayashiDivision of Bacterial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States.
Wei XingDivision of Bacterial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States.
Adam L CohenDivision of Bacterial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, United States.
Wesley H SelfVanderbilt University Medical Center, Nashville, Tennessee, United States.
J Jackson ResserVanderbilt University Medical Center, Nashville, Tennessee, United States.
Cynthia G WhitneyRollins School of Public Health, Emory University, Atlanta, Georgia, United States.
Adrienne BaughmanVanderbilt University Medical Center, Nashville, Tennessee, United States.
Mai KioDepartment of Medicine, Emory University, Atlanta, Georgia, United States.
Carlos G GrijalvaVanderbilt University Medical Center, Nashville, Tennessee, United States.
Jessica TraenknerDepartment of Medicine, Emory University, Atlanta, Georgia, United States.
Nadine RouphaelDepartment of Medicine, Emory University, Atlanta, Georgia, United States.
Joseph A LewnardSchool of Public Health, University of California, Berkeley, Berkeley, California, United States.

Funding

Quantifying the impact of vaccines on antibiotic use for respiratory infections in childrenF31AI174773 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI KING, LAURA · 2023 to 2025
$90k
NIAID NIH HHS F31 AI174773
6 · The paper itself

Abstract

Background: Methods: We estimated serotype distribution and proportions of non-invasive pneumococcal ARIs (AOM [children only], sinusitis, non-bacteremic pneumonia) and IPD attributable to serotypes targeted by each PCV using Markov chain Monte Carlo approaches incorporating data from studies of serotype distribution in ARIs and Active Bacterial Core Surveillance (ABCs) data. We then estimated annual numbers of outpatient-managed pneumococcal ARIs, non-bacteremic pneumococcal pneumonia hospitalizations, and IPD cases potentially preventable by PCVs in the United States by multiplying pneumococcal disease incidence rates by PCV-targeted proportions of disease and vaccine effectiveness estimates. Results: In children, PCV15, PCV20, PCV24, PCV25, and PCV31 serotypes account for 16% (95% confidence interval: 15-17%), 31% (30-32%), 34% (32-35%), 43% (42-44%), and 68% (67-69%) of pneumococcal acute otitis media cases, respectively. In adults, PCV15, PCV20, PCV21, PCV24, PCV25, and PCV31 serotypes account for 43% (38-47%), 52% (47-57%), 69% (64-73%), 65% (61-70%), 62% (57-67%), and 87% (83-90%) of pneumococcal non-bacteremic pneumonia cases. For IPD, 42-85% of pediatric and 42-94% of adult cases were due to PCV-targeted serotypes. PCV-preventable burdens encompassed 270 thousand-3.3 million outpatient-managed ARIs, 2-17 thousand non-bacteremic pneumonia hospitalizations, and 3-14 thousand IPD cases in the United States annually. Conclusions: Across pneumococcal conditions, coverage and preventable burdens were lowest for PCV15 and highest for PCV31, with PCV21 also targeting sizeable burdens of adult disease. Serotype distribution across syndromes may inform vaccine formulations and policy.

Identifiers

PMID39711720
PMCPMC11661329

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.